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Fig. 1 | BMC Medical Genetics

Fig. 1

From: New genetic variant in the SERPINC1 gene: hereditary Antithrombin deficiency case report, familial thrombosis and considerations on genetic counseling

Fig. 1

a. Family tree of the proband (marked with the red arrow); N/T – family members, not tested for p.W221S variant; N/N – family member without p.W221S variant (both allelеs are normal); blue shape filled – family members with the history of thrombosis. B. The fragment of chromatogram showing the sequence of exon 4 of SERPINC1 gene in proband. Sequences made with forward primer (upper picture) and reverse-complement reverse primer (lower picture) are shown. The genetic variant c.662 G > C is marked with blue arrow

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